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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 280760Generated: October 29, 2026

Sodium Bicarbonate → 2-Guanidino-4-(2-hydroxymethyl-4-imidazolyl)thiazole hydrobromide

https://huagongshe.com/reaction/280760

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178419746HCID 178419746—
ReactantHCID 178513045HCID 178513045—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
Product2-Guanidino-4-(2-hydroxymethyl-4-imidazolyl)thiazole hydrobromideHCID 17841971687.6%

Reaction Steps

1.78 g (0.0059 mol) of 2-hydroxymethyl-4-bromoacetylimidazole hydrobromide was dissolved in water and saturated sodium bicarbonate solution was added to precipitate the free base. This material was collected by filtration and dried and combined with 956 mg (0.0081 mol) of amidinothiourea in 60 ml acetone and heated to 70° . After 15 minutes heating a solid formed. The reaction mixture was cooled and the resultant solid was collected by filtration to give 1.65 g (87%) 2-guanidino-4-(2-hydroxymethyl-4-imidazolyl)thiazole hydrobromide, mp>310°. A sample was converted to the free base by dissolving in hot water and adding sodium bicarbonate solid to pH 10 to precipitate 2-guanidino-4-(2-hydroxymethyl-4-imidazolyl)thiazole free base. This material was dried over toluene at high vacuum to give a light tan solid, mp 208°-209° with decomposition. nmr (DMSO-d6) (δ): 7.16 (s, 1H); 6.83 (broad s, 4H) 6.68 (s, 1H); 4.45 (s, 2H); 3.46 (very broad s, 1H). High resolution mass spectrum, calcd for C8H10N6OS: 238.0638; found: 238.0654.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04590299
Source datasetuspto-grants-1986_05
ORD IDord-d8c024e2c82e417db9c76ee7fc064390
Source noteuspto-grants-1986_05